Familial typical migraine: Significant linkage and localization of a gene to Xq24-28

Human Genetics

Volumn 107, Issue 1, 2000, Pages 18-23

  Nyholt, Dale R ^a   Curtain, Robert P ^b   Griffiths, Lyn R ^b  

^a ROCKEFELLER UNIVERSITY   (United States)

^b GRIFFITH UNIVERSITY   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ARTICLE; AUSTRALIA; CAUCASIAN; CHROMOSOME XQ; COMPUTER PROGRAM; FAMILIAL DISEASE; GENETIC LINKAGE; HAPLOTYPE; HUMAN; MIGRAINE; PEDIGREE; PRIORITY JOURNAL;

CHROMOSOME MAPPING; FEMALE; GENETIC MARKERS; HAPLOTYPES; HUMANS; LINKAGE (GENETICS); LOD SCORE; MALE; MIGRAINE DISORDERS; MIGRAINE WITH AURA; MIGRAINE WITHOUT AURA; PEDIGREE; RECOMBINATION, GENETIC; X CHROMOSOME;

EID: 0033880566     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050004     Document Type: Article

References (29)

1. Ferrari MD, Saxena PR (1993) On serotonin and migraine: a clinical and pharmacological review. Cephalalgia 13:151-165
2. Goadsby PJ, Zagami AS, Lambert GA (1991) Neural processing of craniovascular pain: a synthesis of the central structures involved in migraine. Headache 31:365-371
3. Gyapay G, Morissette J, Vignal A, Dib C, Fizames C, Millasseau P, Marc S, Bernardi G, Lathrop M, Weissenbach J (1994) The 1993-94 Genethon human genetic linkage map. Nat Genet 7: 246-339
4. Headache Classification Committee of the International Headache Society (1988) Classification and diagnostic criteria for headache disorders, cranial neuralgias and facial pain. Cephalalgia 8 [Suppl 7]:19-28
5. Honkasalo M-L, Kaprio J, Winter T, Heikkila K, Sillanpaa M, Koskenvuo M (1995) Migraine and concomitant symptoms among 8167 adult twin pairs. Headache 35:70-78
6. Kong A, Cox NJ (1997) Allele-sharing models: LOD scores and accurate linkage tests. Am J Hum Genet 61:1179-1188
7. Kruglyak L, Daly MJ, Reeve-Daly MP, Lander ES (1996) Parametric and non-parametric linkage analysis: a unified multi-point approach. Am J Hum Genet 58:1347-1363
8. Larsson B, Bille B, Pedersen NL (1995) Genetic influence in headaches: a Swedish twin study. Headache 35:513-519
9. Launer LJ, Terwindt GM, Ferrari MD (1999) The prevalence and characteristics of migraine in a population-based cohort: the GEM study. Neurology 53:537-542
10. Milatovich A. Hsieh C-L, Bonaminio G, Tecott L, Julius D, Francke U (1992) Serotonin receptor 1C gene assigned to X chromosome in human (band q24) and mouse (bands D-F4). Hum Mol Genet 1:681-684
11. Nagaraja R, MacMillan S, Jones C, Masisi M, Pengue G, Porta G, Miao S, Casamassimi A, D'Urso M, Brownstein B, Schlessinger D (1998) Integrated YAC/STS physical and genetic map of 22.5 Mb of human Xq24-q26 at 56-kb inter-STS resolution. Genomics 52:247-266
12. Nyholt DR, Lea RA, Goadsby PJ, Brimage PJ, Griffiths LR (1998a) Familial typical migraine: linkage to chromosome 19p13 and evidence for genetic heterogeneity. Neurology 50: 1428-1432
13. Nyholt DR, Dawkins JL, Brimage PJ, Goadsby PJ, Nicholson GA, Griffiths LR (1998b) Evidence for an X-linked genetic component in familial typical migraine. Hum Mol Genet 7:459-463
14. Ophoff RA, Terwindt GM, Vergouwe MN, van Eijk R, Oefner PJ, Hoffman SM, Lamerdin JE, Mohrenweiser HW, Bulman DE, Ferrari M, Haan J, Lindhout D, van Ommen GJ, Hofker MH, Ferrari MD, Frants RR (1996) Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4. Cell 87:543-552
15. Ott J (1986) Linkage probability and its approximate confidence interval under possible heterogeneity. Genet Epidemiol Suppl 1:251-257
16. Palmieri G, Romano G, Casamassimi A, D'Urso M, Little RD, Abidi FE, Schlessinger D, Lagerstrom M, Malmgren H, Steen-Bondeson M-L, Pettersson U, Landegren U (1993) 1.5-Mb YAC contig in Xq28 formatted with sequence-tagged sites and including a region unstable in the clones. Genomics 16:586-592
17. Peroutka SJ (1990) Developments in 5-hydroxytryptamine receptor pharmacology in migraine. Neurol Clin 8:829-838
18. Pilia G, MacMillan S, Nagaraja R, Mumm S, Weissenbach J, Schlessinger D (1996) YAC/STS map of 9 Mb of Xq26 at 100-kb resolution, localizing 6 ESTs, 6 genes, and 32 genetic markers. Genomics 34:55-62
19. Rasmussen BK, Olesen J (1992) Migraine with aura and migraine without aura. An epidemiological study. Cephalalgia 12:221-228
20. Rozen TD, Swanson JW, Stang PE, McDonnell SK, Rocca WA (1999) Increasing incidence of medically recognized migraine headache in a United States population. Neurology 53:1468-1473
21. Russell MB, Olesen J (1993) The genetics of migraine without aura and migraine with aura. Cephalalgia 13:245-248
22. Silberstein SD (1994) Review: serotonin 5-HT and migraine. Headache 34:408-417
23. Silberstein SD, Lipton RB (1994) Overview of diagnosis and treatment of migraine. Neurology 44 [Suppl 7]:S6-S16
24. Stewart WF, Linet MS, Celentano DD, Natta MV, Ziegler D (1991) Age-and sex-specific incidence rates of migraine with and without visual aura. Am J Epidemiol 134:1111-1120
25. Stewart WF, Lipton RB, Celentano DD, Reed ML (1992) Prevalence of migraine headache in the United States. JAMA 267: 64-69
26. Stewart WF, Staffa J, Lipton RB, Ottman R (1997) Familial risk of migraine: a population based study. Ann Neurol 41:166-172
27. Terwilliger JD, Ott J (1994) Handbook of genetic linkage. Johns Hopkins University Press, Baltimore
28. Zhuchenko O, Bailey J, Bonnen P, Ashizawa T, Stockton DW, Amos C, Dobyns WB, Subramony SH, Zoghbi HY, Lee CC (1997) Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel. Nat Genet 15:62-69
29. Zucchi I, Mumm S, Pilia G, Macmillan S, Reinbold R, Susani L, Weissenbach J, Schlessinger D (1996) YAC/STS map across 12 Mb of Xq27 at 25-kb resolution, merging Xq26-qter. Genomics 34:42-54